GlyCosmos Portal

Source	Last Updated
GlyConnect	April 19, 2023
GlycoProtDB	October 1, 2021
GlyGen	June 4, 2024
The O-GlcNAc Database	June 3, 2024
UniProt	June 4, 2024

Displaying entries **13676 - 13700** of **18496** in total

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UniProt ID	Protein Name	Gene Symbol	Organism ▼	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
P48067	Sodium- and chloride-dependent glycine transporter 1	SLC6A9	Homo sapiens (human)	3	2
O14578	Citron Rho-interacting kinase	CIT CRIK KIAA0949 STK21	Homo sapiens (human)	1	2
A0A2U7N6T0	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1	0
A8VYQ6	MHC class I antigen (Fragment)	HLA-B	Homo sapiens (human)	1	0
Q7Z401	C-myc promoter-binding protein	DENND4A IRLB MYCPBP	Homo sapiens (human)	1	2
Q8IXB4	Vitamin K-dependent protein C (Fragment)	PROC1	Homo sapiens (human)	1	0
Q6Y288	Beta-1,3-glucosyltransferase	B3GLCT B3GALTL B3GTL	Homo sapiens (human)	3	6	Axenfeld-Rieger syndrome IGSF1 deficiency syndrome Klippel-Feil syndrome Kuhnt-Junius degeneration Meckel syndrome Peters anomaly Peters plus syndrome Tn polyagglutination syndrome age related macular degeneration anemia atrial heart septal defect 1 atrial heart septal defect 2 atrial heart septal defect 3 atrial heart septal defect 4 atrial heart septal defect 5 atrial heart septal defect 6 atrial heart septal defect 7 atrial heart septal defect 8 atrial heart septal defect 9 atrial heart septal defect autism spectrum disorder autistic disorder autosomal dominant polycystic kidney disease blindness cataract cerebral degeneration cleft lip cleft palate coloboma communicating hydrocephalus congenital hypothyroidism congenital nongoitrous hypothyroidism 1 congenital nongoitrous hypothyroidism 2 congenital nongoitrous hypothyroidism 3 congenital nongoitrous hypothyroidism 4 congenital nongoitrous hypothyroidism 5 congenital nongoitrous hypothyroidism 6 congenital nystagmus congenital ptosis cornea plana craniosynostosis cryptorchidism degeneration of macula and posterior pole depressive disorder dissociated nystagmus epilepsy eye disease glaucoma heart septal defect hydrocephalus hydronephrosis hypoplastic left heart syndrome hypospadias hypothyroidism imperforate anus inguinal hernia intellectual disability isolated cleft palate learning disability macrocytic anemia macular degeneration major depressive disorder melancholic depression microcephaly myopia myxedema obsolete melancholia obstructive hydrocephalus omphalocele optic atrophy patent ductus arteriosus patent foramen ovale pathologic nystagmus placental insufficiency polyhydramnios popliteal pterygium syndrome ptosis pulmonary valve stenosis recurrent corneal erosion renal hypoplasia scoliosis senile degeneration of brain sensorineural hearing loss spina bifida occulta spondylolisthesis spontaneous ocular nystagmus syndactyly trichohepatoenteric syndrome 1 trichohepatoenteric syndrome umbilical hernia ventricular septal defect visual epilepsy
F8VRH0	Poly(rC) binding protein 2 (Fragment)	PCBP2	Homo sapiens (human)	0	1
K7P5Y9	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1	0
Q9Y4R7	Tubulin monoglycylase TTLL3	TTLL3	Homo sapiens (human)	1	1
P01106	Myc proto-oncogene protein	MYC BHLHE39	Homo sapiens (human)	1	1
P28074	Proteasome subunit beta type-5	PSMB5 LMPX MB1 X	Homo sapiens (human)	0	1
P29274	Adenosine receptor A2a	ADORA2A ADORA2	Homo sapiens (human)	1	0
P61088	Ubiquitin-conjugating enzyme E2 N	UBE2N BLU	Homo sapiens (human)	0	1
Q96ED9	Protein Hook homolog 2	HOOK2	Homo sapiens (human)	0	1
Q86VE9	Serine incorporator 5	SERINC5 C5orf12	Homo sapiens (human)	3	0
A1DZU0	MHC class I antigen (Fragment)	HLA-B	Homo sapiens (human)	1	0
Q6P1X5	Transcription initiation factor TFIID subunit 2	TAF2 CIF150 TAF2B	Homo sapiens (human)	1	1
Q3ZCW2	Galectin-related protein	LGALSL GRP	Homo sapiens (human)	1	2
P0DN82	Olfactory receptor 12D1	OR12D1 OR12D1P	Homo sapiens (human)	1	0
H9C8X7	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1	0
P35268	Large ribosomal subunit protein eL22	RPL22	Homo sapiens (human)	0	1
Q99504	Eyes absent homolog 3	EYA3	Homo sapiens (human)	5	3
A0A669KBG0	Proprotein convertase subtilisin/kexin type 9	PCSK9	Homo sapiens (human)	1	0
A0A0A7C5G8	MHC class I antigen (Fragment)	HLA-B	Homo sapiens (human)	1	0

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